Table S3. Details of neoadjuvant chemotherapy post LCRT (n=96).
Characteristics | n (% where applicable) |
---|---|
Reasons for neoadjuvant chemotherapy | |
Persistent radiological CRM positivity | 78 (81.3) |
Organ infiltration requiring extended resection | 6 (6.3) |
Interim chemotherapy | 9 (9.4) |
Threatened radiological CRM | 3 (3.0) |
Regimens used as neoadjuvant | |
mFOLFIRINOX | 54 (56.3) |
CAPOX | 42 (43.7) |
Median number of chemotherapy doses | 4 [1–8] |
Data available for grade 3 and grade 4 toxicities | 78 (81.3) |
Individual toxicities | |
Vomiting | 2 (2.6) |
Oral mucositis | 2 (2.6) |
Diarrhoea | 14 (17.9) |
HFS (grade 2 and grade 3) | 6 (6.3) |
Neutropenia | 14 (17.9) |
Febrile neutropenia | 5 (6.4) |
Anemia | 2 (2.6) |
Non-neutropenic infections | 3 (3.8) |
Fatigue (grade 3) | 2 (2.6) |
Peripheral neuropathy (grade 3) | 4 (5.1) |
Clinico-radiological response rates | |
Complete response | 0 |
Partial response | 35 (36.4) |
Stable disease | 45 (46.9) |
Progressive disease | 8 (8.3) |
Not available | 8 (8.3) |
Curative intent local resection post neoadjuvant chemotherapy | |
Yes | 55 (57.3) |
No | 41 (42.7) |
LCRT, long course chemoradiotherapy; CRM, circumferential margin; HFS, hand-foot syndrome; mFOLFIRINOX, modified 5 fluorouracil-leucovorin-irinotecan-oxaliplatin; CAPOX, capecitabine-oxaliplatin.